Cryopreservation of embryos as a means of germ plasm conservation in sheep.

Embryos were collected from 4 lines of Targhee sheep between 1986 and 1990. The lines were selected for preweaning growth rate (Lines DH and HW) or for multiple births (Line HT); Line C served as an unselected control group. Estrus was synchronized using fluorogestone acetate-impregnated vaginal pessaries, and ewes were superovulated with FSH. Embryos at the morula or blastocyst stage were surgically recovered from mature ewes at Days 5 to 6 and were frozen following morphological evaluation. The overall average number of freezable embryos per collection was 2.9, and did not differ significantly among years or among lines. Of the embryos collected between 1986 and 1988, 92 were transferred to 53 recipients in 1989, producing 53 lambs. Survival rates were 60.9 and 47.8%, respectively, for embryos evaluated as good and fair after thawing. Good-quality blastocysts yielded the highest survival rate (64.4%). Analyses indicated no significant effects of line, developmental stage or embryo evaluation on the incidence of lambing. It was concluded that embryos of morula or blastocyst stage can be successfully frozen for extended periods. The data on embryo yield and survival following cryopreservation were used to calculate numbers of donors needed to preserve and reconstitute a population of specified size.

Effects of maternal and embryonic genotype on prenatal survival in two selected mouse lines.

The effect of fetal and maternal genotype on embryo survival was studied in two lines of mice from the same base population: line E, selected for high embryo survival, and line CN-, selected for small litter size. Embryos were collected at 3.5 days postcoitus from normally mated donors of both lines and were transferred to the uteri of 2.5-day pseudopregnant recipients from each line. The number of embryos recovered and the proportion of those recovered that had been fertilized were greater in line E donors than in line CN- donors (P < .05). Development into blastocysts was slower for CN- embryos. The proportion of recipient females that were pregnant was higher for line E than for line CN- after transfer of line E embryos (P < .005). The same trend was observed following transfer of line CN- embryos (P < .10). Embryos of both lines showed greater survival when transferred to line E recipients than when transferred to line CN- recipients (P < .005), and, within line E recipients, E embryos tended to survive better than did CN- embryos (P < .10). The results suggest that although the genotype of the embryo may play a role, the maternal genotype has greater influence on embryo survival in the two lines of mice.

A simple technique for nonsurgical embryo transfer in mice.

A simple method was developed for nonsurgical transfer of mouse embryos which enabled transfer to both uterine horns. Embryos were picked up in a modified capillary tube and transferred through the cervix into each uterine horn of an unanesthetized mouse. A glass speculum was used to facilitate location of the cervix. The technique was found to be as successful (up to 60% of embryos transferred developed to term) as surgical methods yet was simpler and eliminated surgical trauma to the recipient mouse.